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Tea Polyphenol Inhibits Allostimulation in Mixed Lymphocyte Culture
Green tea polyphenols are known to protect allogenic donor tissues from acute rejection by their recipients. This immunosuppressive effect may be generated by a unique chemical property of the major component, epigallocatechin-o-gallate (EGCG), which can block specific cell surface molecules of the...
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Published in: | Cell transplantation 2007-01, Vol.16 (1), p.75-83 |
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container_title | Cell transplantation |
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creator | Kim, Jong-Yoon Kina, Tatsuo Iwanaga, Yasuhiro Noguchi, Hirofumi Matsumura, Kazuaki Hyon, Suong-Hyu |
description | Green tea polyphenols are known to protect allogenic donor tissues from acute rejection by their recipients. This immunosuppressive effect may be generated by a unique chemical property of the major component, epigallocatechin-o-gallate (EGCG), which can block specific cell surface molecules of the donor tissues. To test this hypothesis, we examined the effects of EGCG on the murine mixed lymphocyte reactions. EGCG treatment of stimulator cells significantly attenuated the proliferation of responder T cells. The proliferation did not recover upon the secondary stimulations by fresh untreated cells or exogenous IL-2. Flow cytometric analyses showed that EGCG treatment decreased the staining intensities of various cell surface molecules including MHC II, which plays a major role in antigen presentation, and B7.1, B7.2, and their ligand, CD28, which are required for costimulatory signals in T-cell activation. These results suggest that an anergic state of alloreactive T cells may be induced by either weakening of antigen signaling or blockage of costimulatory signals with EGCG. Other possible mechanisms behind the immunosuppressive effect and a potential use of EGCG treatment of donor tissues in transplantation medicine are discussed. |
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This immunosuppressive effect may be generated by a unique chemical property of the major component, epigallocatechin-o-gallate (EGCG), which can block specific cell surface molecules of the donor tissues. To test this hypothesis, we examined the effects of EGCG on the murine mixed lymphocyte reactions. EGCG treatment of stimulator cells significantly attenuated the proliferation of responder T cells. The proliferation did not recover upon the secondary stimulations by fresh untreated cells or exogenous IL-2. Flow cytometric analyses showed that EGCG treatment decreased the staining intensities of various cell surface molecules including MHC II, which plays a major role in antigen presentation, and B7.1, B7.2, and their ligand, CD28, which are required for costimulatory signals in T-cell activation. These results suggest that an anergic state of alloreactive T cells may be induced by either weakening of antigen signaling or blockage of costimulatory signals with EGCG. Other possible mechanisms behind the immunosuppressive effect and a potential use of EGCG treatment of donor tissues in transplantation medicine are discussed.</description><identifier>ISSN: 0963-6897</identifier><identifier>EISSN: 1555-3892</identifier><identifier>DOI: 10.3727/000000007783464515</identifier><identifier>PMID: 17436857</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Animals ; Apoptosis ; Catechin - analogs & derivatives ; Catechin - pharmacology ; Cell Proliferation ; Cells, Cultured ; Female ; Flavonoids - pharmacology ; Flow Cytometry ; Immunosuppressive Agents - pharmacology ; Interleukin-2 - immunology ; Lymphocyte Activation - drug effects ; Lymphocyte Culture Test, Mixed ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Phenols - pharmacology ; Plant Extracts - chemistry ; Polyphenols ; Tea - chemistry</subject><ispartof>Cell transplantation, 2007-01, Vol.16 (1), p.75-83</ispartof><rights>2007 Cognizant Comm. Corp.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c517t-a8d9c0cc115b8acf81ff2e413bccf71523b3c9149861c359c02e8d19d86d2a033</citedby><cites>FETCH-LOGICAL-c517t-a8d9c0cc115b8acf81ff2e413bccf71523b3c9149861c359c02e8d19d86d2a033</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.3727/000000007783464515$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.3727/000000007783464515$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,780,784,4024,21966,27853,27923,27924,27925,44945,45333</link.rule.ids><linktorsrc>$$Uhttps://journals.sagepub.com/doi/full/10.3727/000000007783464515?utm_source=summon&utm_medium=discovery-provider$$EView_record_in_SAGE_Publications$$FView_record_in_$$GSAGE_Publications</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17436857$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Jong-Yoon</creatorcontrib><creatorcontrib>Kina, Tatsuo</creatorcontrib><creatorcontrib>Iwanaga, Yasuhiro</creatorcontrib><creatorcontrib>Noguchi, Hirofumi</creatorcontrib><creatorcontrib>Matsumura, Kazuaki</creatorcontrib><creatorcontrib>Hyon, Suong-Hyu</creatorcontrib><title>Tea Polyphenol Inhibits Allostimulation in Mixed Lymphocyte Culture</title><title>Cell transplantation</title><addtitle>Cell Transplant</addtitle><description>Green tea polyphenols are known to protect allogenic donor tissues from acute rejection by their recipients. This immunosuppressive effect may be generated by a unique chemical property of the major component, epigallocatechin-o-gallate (EGCG), which can block specific cell surface molecules of the donor tissues. To test this hypothesis, we examined the effects of EGCG on the murine mixed lymphocyte reactions. EGCG treatment of stimulator cells significantly attenuated the proliferation of responder T cells. The proliferation did not recover upon the secondary stimulations by fresh untreated cells or exogenous IL-2. Flow cytometric analyses showed that EGCG treatment decreased the staining intensities of various cell surface molecules including MHC II, which plays a major role in antigen presentation, and B7.1, B7.2, and their ligand, CD28, which are required for costimulatory signals in T-cell activation. These results suggest that an anergic state of alloreactive T cells may be induced by either weakening of antigen signaling or blockage of costimulatory signals with EGCG. Other possible mechanisms behind the immunosuppressive effect and a potential use of EGCG treatment of donor tissues in transplantation medicine are discussed.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Catechin - analogs & derivatives</subject><subject>Catechin - pharmacology</subject><subject>Cell Proliferation</subject><subject>Cells, Cultured</subject><subject>Female</subject><subject>Flavonoids - pharmacology</subject><subject>Flow Cytometry</subject><subject>Immunosuppressive Agents - pharmacology</subject><subject>Interleukin-2 - immunology</subject><subject>Lymphocyte Activation - drug effects</subject><subject>Lymphocyte Culture Test, Mixed</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Phenols - pharmacology</subject><subject>Plant Extracts - chemistry</subject><subject>Polyphenols</subject><subject>Tea - chemistry</subject><issn>0963-6897</issn><issn>1555-3892</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kU1r3DAQhkVpaDYff6CH4lNvbjT69jEsTbuwpTmkZyGP5awW2dpKNnT_fZ3u0h4CncvA8MwzMC8h74F-4prpO3ourQ0XSkiQb8gKpJQ1Nw17S1a0UbxWptGX5KqU_QvKmXxHLkELrozUK7J-8q56TPF42PkxxWoz7kIbplLdx5jKFIY5uimksQpj9S388l21PQ6HXcLj5Kv1HKc5-xty0btY_O25X5MfD5-f1l_r7fcvm_X9tkYJeqqd6RqkiACyNQ57A33PvADeIvYaJOMtxwZEYxQglwvLvOmg6YzqmKOcX5PNydslt7eHHAaXjza5YP8MUn62Lk8Bo7eUCgWMMdRtK7QDwwQ61EqoRiMwv7g-nlyHnH7Ovkx2CAV9jG70aS5WU240U3oB2QnEnErJvv97GKh9icG-jmFZ-nC2z-3gu38r578vwN0JKO7Z232a87h87n_K3z62jn8</recordid><startdate>200701</startdate><enddate>200701</enddate><creator>Kim, Jong-Yoon</creator><creator>Kina, Tatsuo</creator><creator>Iwanaga, Yasuhiro</creator><creator>Noguchi, Hirofumi</creator><creator>Matsumura, Kazuaki</creator><creator>Hyon, Suong-Hyu</creator><general>SAGE Publications</general><general>SAGE Publishing</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>DOA</scope></search><sort><creationdate>200701</creationdate><title>Tea Polyphenol Inhibits Allostimulation in Mixed Lymphocyte Culture</title><author>Kim, Jong-Yoon ; Kina, Tatsuo ; Iwanaga, Yasuhiro ; Noguchi, Hirofumi ; Matsumura, Kazuaki ; Hyon, Suong-Hyu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c517t-a8d9c0cc115b8acf81ff2e413bccf71523b3c9149861c359c02e8d19d86d2a033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Catechin - analogs & derivatives</topic><topic>Catechin - pharmacology</topic><topic>Cell Proliferation</topic><topic>Cells, Cultured</topic><topic>Female</topic><topic>Flavonoids - pharmacology</topic><topic>Flow Cytometry</topic><topic>Immunosuppressive Agents - pharmacology</topic><topic>Interleukin-2 - immunology</topic><topic>Lymphocyte Activation - drug effects</topic><topic>Lymphocyte Culture Test, Mixed</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Phenols - pharmacology</topic><topic>Plant Extracts - chemistry</topic><topic>Polyphenols</topic><topic>Tea - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Jong-Yoon</creatorcontrib><creatorcontrib>Kina, Tatsuo</creatorcontrib><creatorcontrib>Iwanaga, Yasuhiro</creatorcontrib><creatorcontrib>Noguchi, Hirofumi</creatorcontrib><creatorcontrib>Matsumura, Kazuaki</creatorcontrib><creatorcontrib>Hyon, Suong-Hyu</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Cell transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Kim, Jong-Yoon</au><au>Kina, Tatsuo</au><au>Iwanaga, Yasuhiro</au><au>Noguchi, Hirofumi</au><au>Matsumura, Kazuaki</au><au>Hyon, Suong-Hyu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tea Polyphenol Inhibits Allostimulation in Mixed Lymphocyte Culture</atitle><jtitle>Cell transplantation</jtitle><addtitle>Cell Transplant</addtitle><date>2007-01</date><risdate>2007</risdate><volume>16</volume><issue>1</issue><spage>75</spage><epage>83</epage><pages>75-83</pages><issn>0963-6897</issn><eissn>1555-3892</eissn><abstract>Green tea polyphenols are known to protect allogenic donor tissues from acute rejection by their recipients. This immunosuppressive effect may be generated by a unique chemical property of the major component, epigallocatechin-o-gallate (EGCG), which can block specific cell surface molecules of the donor tissues. To test this hypothesis, we examined the effects of EGCG on the murine mixed lymphocyte reactions. EGCG treatment of stimulator cells significantly attenuated the proliferation of responder T cells. The proliferation did not recover upon the secondary stimulations by fresh untreated cells or exogenous IL-2. Flow cytometric analyses showed that EGCG treatment decreased the staining intensities of various cell surface molecules including MHC II, which plays a major role in antigen presentation, and B7.1, B7.2, and their ligand, CD28, which are required for costimulatory signals in T-cell activation. These results suggest that an anergic state of alloreactive T cells may be induced by either weakening of antigen signaling or blockage of costimulatory signals with EGCG. Other possible mechanisms behind the immunosuppressive effect and a potential use of EGCG treatment of donor tissues in transplantation medicine are discussed.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>17436857</pmid><doi>10.3727/000000007783464515</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Apoptosis Catechin - analogs & derivatives Catechin - pharmacology Cell Proliferation Cells, Cultured Female Flavonoids - pharmacology Flow Cytometry Immunosuppressive Agents - pharmacology Interleukin-2 - immunology Lymphocyte Activation - drug effects Lymphocyte Culture Test, Mixed Mice Mice, Inbred BALB C Mice, Inbred C57BL Phenols - pharmacology Plant Extracts - chemistry Polyphenols Tea - chemistry |
title | Tea Polyphenol Inhibits Allostimulation in Mixed Lymphocyte Culture |
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